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Excitatory amino acids mediate responses elicited in vitro by stimulation of cortical afferents to reticularis thalami neurons of the rat.
- Source :
-
Neuroscience [Neuroscience] 1989; Vol. 33 (2), pp. 275-83. - Publication Year :
- 1989
-
Abstract
- The effects of the excitatory amino acids on the nucleus reticularis thalami were examined by intracellular recordings from rat thalamic slices. Non-N-methyl-D-aspartate receptor agonists and glutamate induced a membrane depolarization and a reduction in input resistance, while N-methyl-D-aspartate and aspartate induced a prolonged discharge, which in some neurons took the form of a burst firing associated with an apparent increase in membrane input resistance. Both the N-methyl-D-aspartate and the aspartate effects were blocked by D-2-amino-5-phosphonovalerate, while the effects of glutamate, kainate and quisqualate were not. The excitatory postsynaptic potential evoked by corticothalamic fiber stimulation shows two components: an early, short-lasting, 2-amino-5-phosphonovalerate-insensitive portion, and a late, 2-amino-5-phosphonovalerate-sensitive decay phase. It is suggested that glutamate acts in nucleus reticularis thalami cells preferentially on the non-N-methyl-D-aspartate receptors, while aspartate shows an N-methyl-D-aspartate-like effect. The two excitatory amino acids glutamate and aspartate play a determinant role in the modulation of thalamic activity driven by corticothalamic projection.
- Subjects :
- 2-Amino-5-phosphonovalerate pharmacology
Action Potentials drug effects
Animals
In Vitro Techniques
N-Methylaspartate
Rats
Rats, Inbred Strains
Thalamus drug effects
Amino Acids pharmacology
Aspartic Acid analogs & derivatives
Aspartic Acid pharmacology
Cerebral Cortex physiology
Thalamus physiology
Subjects
Details
- Language :
- English
- ISSN :
- 0306-4522
- Volume :
- 33
- Issue :
- 2
- Database :
- MEDLINE
- Journal :
- Neuroscience
- Publication Type :
- Academic Journal
- Accession number :
- 2576112
- Full Text :
- https://doi.org/10.1016/0306-4522(89)90207-8